
Clinical Affairs
2 days ago
- Age limit:20 to 30.
- Clinical Study Design & Execution: Leading the design and implementation of clinical study protocols and monitoring their progress.
- Regulatory Compliance: Ensuring all activities, from clinical trials to post-market evaluations, adhere to regulatory requirements and guidelines (e.g., FDA regulations, GCP).
- Data Management & Analysis: Overseeing the collection, interpretation, and reporting of clinical data to ensure its accuracy and integrity.
- Cross-Functional Collaboration: Working with various departments, including R&D, regulatory affairs, quality, risk management, and marketing, to integrate clinical strategy with product development.
- Investigator & Site Management: Recruiting and managing relationships with clinical trial investigators and research sites.
- Regulatory Submissions: Preparing the clinical sections of documents for regulatory submissions and providing clinical information for other reports.
- Product Lifecycle Support: Providing scientific evidence and insights throughout the product's lifecycle, including during post-market surveillance.
Job Types: Full-time, Permanent, Fresher
Pay: ₹38, ₹52,536.72 per month
Benefits:
- Food provided
Work Location: In person
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